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Journal of Clinical Medicine|November 28, 2018
Efficacy and Safety of Denosumab Therapy for Osteogenesis Imperfecta Patients with Osteoporosis-Case SeriesTsukasa Kobayashi, Yukio Nakamura, Takako Suzuki, et al.
European Journal of Endocrinology|October 25, 2014
Heterozygous defects in PAX6 gene and congenital hypopituitarismMasaki Takagi, Keisuke Nagasaki, Ikuma Fujiwara, et al.
BMC Research Notes|February 9, 2018
Double non-contiguous fractures in a patient with spondylo-epiphyseal dysplasia with spinal ankylosis treated with open and percutaneous spinal fixation technique: a case reportTakahiro Ushijima, Kenichi Kawaguchi, Tadashi Matsumoto, et al.
Plos One|October 3, 2012
Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarismMasaki Takagi, Tomohiro Ishii, Mikako Inokuchi, et al.
European Journal of Endocrinology|May 27, 2017
Genetic defects in pediatric-onset adrenal insufficiency in JapanNaoko Amano, Satoshi Narumi, Mie Hayashi, et al.
European Journal of Pediatrics|January 7, 2014
Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literatureTaichi Kitaoka, Yoko Miyoshi, Noriyuki Namba, et al.
American Journal of Medical Genetics. Part A|August 12, 2011
Heterozygous C-propeptide mutations in COL1A1: osteogenesis imperfecta type IIC and dense bone variantMasaki Takagi, Naoaki Hori, Yasutsugu Chinen, et al.
Plos One|May 23, 2012
A novel mutation in LEPRE1 that eliminates only the KDEL ER- retrieval sequence causes non-lethal osteogenesis imperfectaMasaki Takagi, Tomohiro Ishii, Aileen M Barnes, et al.
Pediatric Radiology|February 13, 2016
Criteria for radiologic diagnosis of hypochondroplasia in neonatesTomoko Saito, Keisuke Nagasaki, Gen Nishimura, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of a potent and short-acting oral calcilytic with a pulsatile secretion of parathyroid hormoneYuko Shinagawa, Teruhiko Inoue, Takeo Katsushima, et al.
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